Stryker GmbH: Medical Device Recall in 2024 - (Recall #: Z-2219-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System.

Product Classification:

Class II

Date Initiated: May 9, 2024

Date Posted: July 3, 2024

Recall Number: Z-2219-2024

Event ID: 94721

Reason for Recall:

The adjustment ring on the device may become loose resulting in the wire tension not being able to be set correctly.

Status: Ongoing

Product Quantity: 39 devices

Code Information:

Lot #J43995, UDI-DI 07613252611035.

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, GA, KY, MA, MI, NE, NJ, OH, OR, and TX. The countries of Germany, Japan, Netherlands, and United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated